Product image of Keplat (Ketoprofen) supplied by GNH India

Keplat

Active Ingredient:
Ketoprofen
Origin:
EU

Keplat (Ketoprofen)

Ketoprofen, the active ingredient in Keplat, is a nonsteroidal anti-inflammatory drug (NSAID) presented as a transdermal patch for topical use. It is employed to relieve mild to moderate pain, reduce inflammation, and improve function in inflammatory musculoskeletal conditions such as arthritis.

GNH India supplies Keplat as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, pharmacies and clinics worldwide. The company adheres to stringent quality standards and provides reliable sourcing for healthcare providers across multiple regions. Keplat is manufactured under EU GMP guidelines and distributed through a secure logistics network.

Manufacturer / TM Owner

Hisamitsu Italia S.R.L.

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Indications & Clinical Uses

  • Ketoprofen is an NSAID that reduces inflammation and pain in musculoskeletal disorders.
  • Mild to moderate pain: Provides analgesic relief by decreasing prostaglandin‑mediated nociception.
  • Inflammatory musculoskeletal conditions: Diminishes swelling and improves joint mobility through COX inhibition.
  • Arthritis: Alleviates chronic joint discomfort and stiffness associated with osteo‑ and rheumatoid arthritis.

How It Works

  • Ketoprofen non‑selectively inhibits cyclooxygenase‑1 and cyclooxygenase‑2 enzymes, leading to reduced synthesis of prostaglandins that mediate inflammation, pain, and fever. The lowered prostaglandin levels result in decreased vascular permeability, edema, and sensitization of nociceptors, producing its analgesic and anti‑inflammatory effects when applied transdermally.

Side Effects

Ketoprofen may cause a range of adverse reactions, from mild skin irritation to rare systemic events.

Common Side Effects

  • Local skin irritation: redness, itching, or burning at the application site.
  • Headache: mild to moderate intensity.
  • Gastrointestinal discomfort: nausea or dyspepsia.
  • Dizziness: transient light‑headedness.
  • Pruritus: generalized itching.
  • Mild edema: localized swelling.

Serious or Rare Side Effects

  • Severe cutaneous reactions: Stevens‑Johnson syndrome or toxic epidermal necrolysis.
  • Hepatic injury: elevated liver enzymes or hepatitis.
  • Renal impairment: reduced kidney function or acute renal failure.
  • Cardiovascular events: increased risk of myocardial infarction or stroke.
  • Gastrointestinal ulceration or bleeding.
  • Anaphylaxis: systemic allergic reaction with respiratory distress.

Precautions & Warnings

  • When using Keplat, consider the following safety measures.
  • Assess renal function: monitor in patients with existing kidney disease.
  • Evaluate hepatic status: use cautiously in individuals with liver impairment.
  • Avoid in known hypersensitivity: contraindicated for patients allergic to ketoprofen or other NSAIDs.
  • Limit use in cardiovascular disease: weigh thrombotic risk in patients with heart conditions.
  • Use with caution in pregnancy: safety not established, avoid unless clearly needed.
  • Store at room temperature: keep in the original packaging, protect from moisture and direct sunlight.

Avoid Interactions

Ketoprofen can interact with several drug classes; monitoring is essential.

Major Interactions (Avoid)

  • Anticoagulants (e.g., warfarin): increased bleeding risk.
  • Other NSAIDs or aspirin: heightened gastrointestinal toxicity.
  • Corticosteroids: additive ulcerogenic effect.
  • ACE inhibitors or ARBs: potential reduction in renal function.
  • Lithium: elevated serum lithium levels.
  • Methotrexate: reduced clearance leading to toxicity.

Moderate Interactions (Monitor Closely)

  • Selective serotonin reuptake inhibitors (SSRIs): modest increase in bleeding.
  • Diuretics: possible renal function alteration.
  • Antihypertensives: may blunt blood pressure control.
  • Digoxin: potential for increased serum concentrations.
  • Oral hypoglycemics: may affect glucose control.

Frequently Asked Questions

Keplat is a transdermal patch that contains ketoprofen, an NSAID indicated for the relief of mild to moderate pain, reduction of inflammation, and improvement of joint function in conditions such as arthritis and other inflammatory musculoskeletal disorders.

Ketoprofen works by non‑selectively inhibiting the cyclooxygenase‑1 and cyclooxygenase‑2 enzymes, which reduces the production of prostaglandins. Lower prostaglandin levels diminish inflammation, swelling, and the sensitisation of pain receptors, providing analgesic and anti‑inflammatory effects.

The specific dose and frequency of Keplat are determined by the prescribing healthcare professional based on the individual’s condition, severity of symptoms, and overall health status. Patients should follow the prescriber’s instructions and not adjust the dose on their own.

Safety data for ketoprofen use in pregnancy and lactation are limited. It is generally advised to avoid Keplat during pregnancy, especially in the third trimester, and to use it only if the potential benefit outweighs the risk. Breastfeeding mothers should consult their physician before use.

To order Keplat, submit an enquiry on the product page at gnhindia.com, specifying the required quantity. GNH India works with hospitals, pharmacies, and procurement teams worldwide, verifies trade or institutional credentials, and then provides pricing, availability, shipping details, and any necessary import documentation.

Keplat delivers ketoprofen via a transdermal patch, offering localized drug delivery that may reduce systemic gastrointestinal exposure compared with oral NSAIDs like ibuprofen. Both belong to the same drug class and share similar mechanisms, but the patch formulation can provide steady plasma levels and convenient once‑daily application.

Keplat should be stored at room temperature, below 25 °C, in its original packaging. Keep the patches away from moisture, direct sunlight, and excessive heat. Do not freeze the product, and ensure the packaging remains sealed until use.

Keplat is applied to clean, dry, hair‑free skin on the intended area. The patch is usually worn for a prescribed period, often 12–24 hours, after which it should be removed and discarded. Follow the healthcare provider’s instructions regarding site rotation and duration of use.

Serious risks include severe skin reactions such as Stevens‑Johnson syndrome, hepatic injury, renal impairment, cardiovascular events like myocardial infarction or stroke, gastrointestinal ulceration or bleeding, and rare cases of anaphylaxis. Patients should seek immediate medical attention if they experience any of these symptoms.

Keplat is contraindicated in individuals with known hypersensitivity to ketoprofen or any NSAID, those with active peptic ulcer disease, severe heart failure, uncontrolled hypertension, significant renal or hepatic impairment, and in the third trimester of pregnancy. Consultation with a healthcare professional is essential before starting therapy.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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